Template:Genetic: Difference between revisions
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:[[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | [[Trisomy 21]] | [[Trisomy 18]] | [[Trisomy X]] | [[Monosomy]] | [[Fragile X Syndrome|Fragile X]] | [[Williams_Syndrome|Williams]] | [[Philadelphia chromosome]] | [[Abnormal_Development_-_Hydatidiform_Mole|Hydatidiform Mole]] | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]] | :[[Abnormal Development - Genetic|'''Genetic Links''']]: [[Abnormal Development - Genetic|Introduction]] | [[Genetic risk maternal age]] | [[Trisomy 21]] | [[Trisomy 18]] | [[Trisomy 13]] | [[Trisomy X]] | [[Monosomy]] | [[Fragile X Syndrome|Fragile X]] | [[Williams_Syndrome|Williams]] | [[Philadelphia chromosome]] | [[Abnormal_Development_-_Hydatidiform_Mole|Hydatidiform Mole]] | [[Prenatal Diagnosis]] | [[Neonatal Diagnosis]] | [[International Classification of Diseases]] | [[Molecular Development - Genetics]] | ||
<noinclude>[[Category:Template]]</noinclude> | <noinclude>[[Category:Template]]</noinclude> | ||
[[Category:Genetic Abnormalities]] [[Category:Abnormal Development]] | [[Category:Genetic Abnormalities]] [[Category:Abnormal Development]] | ||
Revision as of 17:36, 21 February 2015
- Genetic Links: Introduction | Genetic risk maternal age | Trisomy 21 | Trisomy 18 | Trisomy 13 | Trisomy X | Monosomy | Fragile X | Williams | Philadelphia chromosome | Hydatidiform Mole | Prenatal Diagnosis | Neonatal Diagnosis | International Classification of Diseases | Molecular Development - Genetics
